510(k) K243752 ยท LRK Device, Anti-Snoring
Double Tube Herbst Appliance
| Applicant | The Tmj Clinic PC, Portland OR, US |
| Decision | Substantially Equivalent, Sep 17, 2025 |
| Received | Dec 5, 2024 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K243752
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.